SEARCH OUR PRODUCT CATALOG

VPS8-NPHP3 Fusion FISH Probe

The VPS8-NPHP3 Fusion FISH Probe is used to confirm a fusion of the VPS8 and NPHP3 genes. The fusion of the VPS8 and NPHP3 genes has been associated with Lung Squamous Cell Carcinoma. These probes are FISH confirmed on normal peripheral blood in both interphase nuclei and metaphase spreads before shipment. Typical turnaround time for this product is 7-14 days after purchase.

** This product is for in vitro and research use only. This product is not intended for diagnostic use. Please note that both genes fall on the same chromosome and inter-chromosomal detection may be difficult to detect depending on the genes proximity to one another. Please consult our support staff before ordering this product to ensure that the probe can be designed to meet your specific needs.

Turnaround Time: 7-10 Business Days    Shipping Time: 1-2 Day Expedited Shipping

SKU Test Kits Buffer Dye Color Order Now
VPS8-NPHP3-20-ORGR  (Standard Design) 20 (40 μL) 200 μL
VPS8-NPHP3-20-RERE 20 (40 μL) 200 μL
VPS8-NPHP3-20-REOR 20 (40 μL) 200 μL
VPS8-NPHP3-20-REGO 20 (40 μL) 200 μL
VPS8-NPHP3-20-REGR 20 (40 μL) 200 μL
VPS8-NPHP3-20-REAQ 20 (40 μL) 200 μL
VPS8-NPHP3-20-ORRE 20 (40 μL) 200 μL
VPS8-NPHP3-20-OROR 20 (40 μL) 200 μL
VPS8-NPHP3-20-ORGO 20 (40 μL) 200 μL
VPS8-NPHP3-20-ORAQ 20 (40 μL) 200 μL
VPS8-NPHP3-20-GORE 20 (40 μL) 200 μL
VPS8-NPHP3-20-GOOR 20 (40 μL) 200 μL
VPS8-NPHP3-20-GOGO 20 (40 μL) 200 μL
VPS8-NPHP3-20-GOGR 20 (40 μL) 200 μL
VPS8-NPHP3-20-GOAQ 20 (40 μL) 200 μL
VPS8-NPHP3-20-GRRE 20 (40 μL) 200 μL
VPS8-NPHP3-20-GROR 20 (40 μL) 200 μL
VPS8-NPHP3-20-GRGO 20 (40 μL) 200 μL
VPS8-NPHP3-20-GRGR 20 (40 μL) 200 μL
VPS8-NPHP3-20-GRAQ 20 (40 μL) 200 μL
VPS8-NPHP3-20-AQRE 20 (40 μL) 200 μL
VPS8-NPHP3-20-AQOR 20 (40 μL) 200 μL
VPS8-NPHP3-20-AQGO 20 (40 μL) 200 μL
VPS8-NPHP3-20-AQGR 20 (40 μL) 200 μL
VPS8-NPHP3-20-AQAQ 20 (40 μL) 200 μL

VPS8 Gene Summary

The VPS8, CORVET Complex Subunit (VPS8) gene is located on chr3 :184529930-184770402 at 3q27.2.

Gene Name: VPS8, CORVET Complex Subunit

Chromosome: CHR3: 184529930 -184770402

Locus: 3q27.2

NPHP3 Gene Summary

This gene encodes a protein containing a coiled-coil (CC) domain, a tubulin-tyrosine ligase (TTL) domain, and a tetratrico peptide repeat (TPR) domain. The encoded protein interacts with nephrocystin, it is required for normal ciliary development, and it functions in renal tubular development. Mutations in this gene are associated with nephronophthisis type 3, and also with renal-hepatic-pancreatic dysplasia, and Meckel syndrome type 7. Naturally occurring read-through transcripts exist between this gene and the downstream ACAD11 (acyl-CoA dehydrogenase family, member 11) gene. [provided by RefSeq, Feb 2011]

Gene Name: Nephrocystin 3

Chromosome: CHR3: 132399452 -132441303

Locus: 3q22.1

Gene Diseases

The VPS8 NPHP3 Fusion has been associated with the following diseases:

Disease Name
Lung Squamous Cell Carcinoma

FISH Probe Protocols

Protocol, Procedure, or Form Name Last Modified Download

Customer Publications

There are currently no FISH related publications for this probe.